Canonical Allele Identifier: CA1610027650

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556037_10556043delinsAGGGGGC , CM000668.2:g.10556037_10556043delinsAGGGGGC	GRCh38
NC_000006.11:g.10556270_10556276delinsAGGGGGC , CM000668.1:g.10556270_10556276delinsAGGGGGC	GRCh37
NC_000006.10:g.10664256_10664262delinsAGGGGGC	NCBI36
NG_007469.3:g.68815_68821delinsAGGGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.-387_-381delinsAGGGGGC MANE Plus Clinical	ENSP00000314844.3:n.-387_-381delinsAGGGGGC
ENST00000397423.7:n.484+27196_484+27202delinsAGGGGGC
ENST00000495262.7:c.925+26201_925+26207delinsAGGGGGC MANE Select	ENSP00000419411.2:n.925+26201_925+26207delinsAGGGGGC
ENST00000316170.7:c.-387_-381delinsAGGGGGC	ENSP00000314844.3:n.-387_-381delinsAGGGGGC
ENST00000379597.7:c.925+26201_925+26207delinsAGGGGGC	ENSP00000368917.3:n.925+26201_925+26207delinsAGGGGGC
ENST00000397423.6:n.484+27196_484+27202delinsAGGGGGC
ENST00000410107.5:c.67+46879_67+46885delinsAGGGGGC	ENSP00000386321.1:n.67+46879_67+46885delinsAGGGGGC
ENST00000461400.1:n.25+26201_25+26207delinsAGGGGGC
ENST00000474518.1:n.508+27196_508+27202delinsAGGGGGC
ENST00000475577.5:n.254+28377_254+28383delinsAGGGGGC
ENST00000485764.1:n.40+26201_40+26207delinsAGGGGGC
ENST00000489225.5:n.283+63106_283+63112delinsAGGGGGC
ENST00000489819.5:n.175+34443_175+34449delinsAGGGGGC
ENST00000495262.5:c.925+26201_925+26207delinsAGGGGGC	ENSP00000419411.1:n.925+26201_925+26207delinsAGGGGGC
NM_001491.2:c.-387_-381delinsAGGGGGC	NP_001482.1:n.-387_-381delinsAGGGGGC
NM_145649.4:c.925+26201_925+26207delinsAGGGGGC	NP_663624.1:n.925+26201_925+26207delinsAGGGGGC
XM_005248997.2:c.-387_-381delinsAGGGGGC	XP_005249054.1:n.-387_-381delinsAGGGGGC
XM_005248999.2:c.694+26201_694+26207delinsAGGGGGC	XP_005249056.1:n.694+26201_694+26207delinsAGGGGGC
XM_006715052.2:c.925+26201_925+26207delinsAGGGGGC	XP_006715115.1:n.925+26201_925+26207delinsAGGGGGC
XM_006715053.2:c.*79_*85delinsAGGGGGC	XP_006715116.1:n.*79_*85delinsAGGGGGC
XM_011514465.1:c.926-17093_926-17087delinsAGGGGGC	XP_011512767.1:n.926-17093_926-17087delinsAGGGGGC
XM_011514467.1:c.694+26201_694+26207delinsAGGGGGC	XP_011512769.1:n.694+26201_694+26207delinsAGGGGGC
XR_926136.1:n.1476+26201_1476+26207delinsAGGGGGC
XM_005248997.3:c.-387_-381delinsAGGGGGC	XP_005249054.1:n.-387_-381delinsAGGGGGC
XM_006715052.3:c.925+26201_925+26207delinsAGGGGGC	XP_006715115.1:n.925+26201_925+26207delinsAGGGGGC
XR_002956275.1:n.1476+26201_1476+26207delinsAGGGGGC
XR_926136.2:n.1474+26201_1474+26207delinsAGGGGGC
NM_001374747.1:c.925+26201_925+26207delinsAGGGGGC	NP_001361676.1:n.925+26201_925+26207delinsAGGGGGC
NM_001491.3:c.-387_-381delinsAGGGGGC MANE Plus Clinical	NP_001482.1:n.-387_-381delinsAGGGGGC
NM_145649.5:c.925+26201_925+26207delinsAGGGGGC MANE Select	NP_663624.1:n.925+26201_925+26207delinsAGGGGGC